Quality Professional - Biotech and Rare Diseases
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Værløse
Are you ready to play a crucial role in ensuring the quality and safety of our products for patients worldwide? Our department is in an exciting transition towards modern technology with many ongoing projects providing opportunities for impacting future production and personal development. Do you thrive in a challenging and ever-changing environment? If yes, then you may be our new colleague in Biotech and Rare Disease QA. Located in Værløse (assembly and packaging) and Gentofte (packaging). The position
As a Quality Assurance (QA) professional you are the gatekeeper for GMP compliance. After a period of introduction and training it will be one of your primary responsibilities to ensure compliance through review of batch documentation and status assignment of assembly and packaging orders according to GMP and our Standard Operating Procedures (SOP). Based on your experience, future tasks can entail quality assurance of our many exciting validation projects. To succeed in this job, it is important to have a close and good collaboration with our production and being able to communicate with a wide range of people. Furthermore, performing QA oversight by being present in our production facilities. As part of the QA team, you will have the opportunity to work with highly skilled people and get a solid understanding of GMP and manufacturing processes in a packaging department. The work environment is informal, and the team is characterized by a high-quality mind-set and a cooperative spirit. Qualifications You have a master’s degree in pharmacy, engineering or similar. You have preferably GMP experience from the pharmaceutical industry. You communicate clearly in English, Danish skills will be a big advantage. It will be an advantage if you have some level of IT flair and knowledge of digitalization tools, as we are facing a lot of new exciting opportunities to improve our processes through digitalization. You demonstrate great communication and collaboration skills. Your drivers are a great personal commitment and accountability in every aspect of your work. We urge you to apply no matter your previous experience. Both newcomers and very experienced candidates are more than welcome to apply. We have great opportunities for personal and professional development for all. About the department
We are a diverse department with 25 employees divided into two areas within Biotech and Rare Disease QA. We are responsible for the quality assurance of our pharmaceutical products of assembled and finished packed products. You will become part of a dedicated team of academics in a casual atmosphere and where we take good care of each other. The team covers two separate packaging departments located in Værløse (assembly and packaging) and Gentofte (packaging). Our department is in an exciting transition towards modern technology with many ongoing projects providing opportunities for impacting future production and personal development. Working at Novo Nordisk At Novo Nordisk your skills, dedication and ambition help us change lives for the better. In return we offer you a chance to work with highly skilled people and benefit from a wide range of possibilities for personal and professional development.
Contact For further information, please contact Maryam Mazari at +45 3448 0569 in the period 7th-25th of August 2023 or Benedicte Hvidberg at +45 3079 2145. Deadline
September 15th 2023. Feel free to submit your application in Danish or English. Please note that applications will be reviewed continuously, and interviews will be planned as soon as suitable candidates have been identified. You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume or CV. To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.
As a Quality Assurance (QA) professional you are the gatekeeper for GMP compliance. After a period of introduction and training it will be one of your primary responsibilities to ensure compliance through review of batch documentation and status assignment of assembly and packaging orders according to GMP and our Standard Operating Procedures (SOP). Based on your experience, future tasks can entail quality assurance of our many exciting validation projects. To succeed in this job, it is important to have a close and good collaboration with our production and being able to communicate with a wide range of people. Furthermore, performing QA oversight by being present in our production facilities. As part of the QA team, you will have the opportunity to work with highly skilled people and get a solid understanding of GMP and manufacturing processes in a packaging department. The work environment is informal, and the team is characterized by a high-quality mind-set and a cooperative spirit. Qualifications
We are a diverse department with 25 employees divided into two areas within Biotech and Rare Disease QA. We are responsible for the quality assurance of our pharmaceutical products of assembled and finished packed products. You will become part of a dedicated team of academics in a casual atmosphere and where we take good care of each other. The team covers two separate packaging departments located in Værløse (assembly and packaging) and Gentofte (packaging). Our department is in an exciting transition towards modern technology with many ongoing projects providing opportunities for impacting future production and personal development. Working at Novo Nordisk At Novo Nordisk your skills, dedication and ambition help us change lives for the better. In return we offer you a chance to work with highly skilled people and benefit from a wide range of possibilities for personal and professional development.
Contact For further information, please contact Maryam Mazari at +45 3448 0569 in the period 7th-25th of August 2023 or Benedicte Hvidberg at +45 3079 2145. Deadline
September 15th 2023. Feel free to submit your application in Danish or English. Please note that applications will be reviewed continuously, and interviews will be planned as soon as suitable candidates have been identified. You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume or CV. To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.
Information og data
Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i Værløse.
Jobbet er oprettet på vores service den 12.7.2023, men kan have været deaktiveret og genaktiveret igen.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
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- Værløse
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